Canonical Allele Identifier: CA9063114
Gene: AMH HGNC NCBI

Linked Data

ClinVar Variation Id: 1593294
ClinVar RCV Id: RCV002112770
dbSNP Id: rs368432946
ExAC: 19:2251835 C / T
gnomAD v2: 19-2251835-C-T
gnomAD v3: 19-2251836-C-T
gnomAD v4: 19-2251836-C-T
MyVariant Identifiers: chr19:g.2251835C>T (hg19) chr19:g.2251836C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.2251836C>T , CM000681.2:g.2251836C>T GRCh38
NC_000019.9:g.2251835C>T , CM000681.1:g.2251835C>T GRCh37
NC_000019.8:g.2202835C>T NCBI36
NG_012190.1:g.7723C>T
NG_032853.1:g.9588G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000221496.5:c.1562C>T MANE Select ENSP00000221496.2:p.Ala521Val
ENST00000221496.4:c.1562C>T ENSP00000221496.2:p.Ala521Val
NM_000479.3:c.1562C>T NP_000470.2:p.Ala521Val
NM_000479.4:c.1562C>T NP_000470.2:p.Ala521Val
NM_000479.5:c.1562C>T MANE Select NP_000470.3:p.Ala521Val
Search 100 bp 5'
Search 100 bp 3'